Filter By “Clinical Trials”

Over the last three years, the proliferation of real-world data at scale has dramatically changed how researchers are thinking about study design, operations, and execution – and the role digital patient data can play. We believe that over the next five years, tokenized clinical trials will be critical to reducing study costs and a force multiplier for accelerating therapeutic innovations for patients. Read this blog post to learn more about about vision and investment in trial tokenization.

When it comes to recruiting patients for clinical trials and collecting the necessary data to assess the impact and safety of novel therapies, trial sponsors and sites are facing greater challenges than ever before.

Increase every clinical trial's full potential with connected data and research-grade insights.

For decades the best practices of clinical research involved rigidly designed, prospective randomized controlled trials (RCTs). While that remains the case in many scenarios, these kinds of trials collected data under ideal conditions and did not always reflect the routine clinical practice settings they are meant to inform. Over the last decade, as real-world data methodology advances and related regulatory guidance has matured it has allowed us to generate the evidence needed for strategy and decision making within development itself.

Despite high effectiveness of COVID-19 vaccines in the real-world, there have been cases of fully vaccinated patients contracting COVID.

A biopharma company was conducting a Phase III study to assess the safety and effectiveness of a new COVID-19 vaccine. They needed to identify and connect to real-world data sources that would enable observation of infection rates and adverse events beyond the period of the trial.

Clinical Trials are some of the world's most expensive data silos. Learn how trial tokenization bridges the gap between trial data and real-world data.

Clinical trial data can be tokenized and connected to valuable, fit for purpose real-world data (RWD) in a privacy-preserving way before, during & after the trial.  

This webinar examines how enriching oncology clinical trials with real-world data generates deeper insights and improves operational efficiency to achieve better patient outcomes.